NDC 77892-0005 Creamol Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
77892-0005
Proprietary Name:
Creamol Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laber Kimya Ar-ge Sanayi Ticaret - Levent Kahriman
Labeler Code:
77892
Start Marketing Date: [9]
08-24-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 77892-0005-1

Package Description: 80 mg in 1 POUCH

NDC Code 77892-0005-2

Package Description: 150 mg in 1 POUCH

Product Details

What is NDC 77892-0005?

The NDC code 77892-0005 is assigned by the FDA to the product Creamol Alcohol Wipes which is product labeled by Laber Kimya Ar-ge Sanayi Ticaret - Levent Kahriman. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 77892-0005-1 80 mg in 1 pouch , 77892-0005-2 150 mg in 1 pouch . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Creamol Alcohol Wipes?

Used for hand and skin cleaning. Open the label and take one. Gently wipe your hands with an antibacterial wipe. It does not require rinsing after use.

Which are Creamol Alcohol Wipes UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Creamol Alcohol Wipes Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".